scholarly journals Expression of Wnt ligands and Frizzled receptors in colonic mucosa and in colon carcinoma

2002 ◽  
Vol 55 (4) ◽  
pp. 220-226 ◽  
Author(s):  
R F Holcombe
2019 ◽  
Author(s):  
Abdulmajeed Fahad Alrefaei ◽  
Andrea E. Münsterberg ◽  
Grant N. Wheeler

AbstractWnt/FZD signalling activity is required for spinal cord development, including the dorsal-ventral patterning of the neural tube, where it affects proliferation and specification of neurons. Wnt ligands initiate canonical, β-catenin-dependent, signaling by binding to Frizzled receptors. However, in many developmental contexts the cognate FZD receptor for a particular Wnt ligand remains to be identified. Here, we characterized FZD10 expression in the dorsal neural tube where it overlaps with both Wnt1 and Wnt3a, as well as markers of dorsal progenitors and interneurons. We show FZD10 expression is sensitive to Wnt1, but not Wnt3a expression, and FZD10 plays a role in neural tube patterning. Knockdown approaches show that Wnt1 induced ventral expansion of dorsal neural markes, Pax6 and Pax7, requires FZD10. In contrast, Wnt3a induced dorsalization of the neural tube is not affected by FZD10 knockdown. Gain of function experiments show that FZD10 is not sufficient on its own to mediate Wnt1 activity in vivo. Indeed excess FZD10 inhibits the dorsalizing activity of Wnt1. However, addition of the Lrp6 co-receptor dramatically enhances the Wnt1/FZD10 mediated activation of dorsal markers. This suggests that the mechanism by which Wnt1 regulates proliferation and patterning in the neural tube requires both FZD10 and Lrp6.


2007 ◽  
Vol 31 (1) ◽  
pp. 76-84 ◽  
Author(s):  
Maria Benevolo ◽  
Marcella Mottolese ◽  
Giulia Piperno ◽  
Isabella Sperduti ◽  
Antonio Cione ◽  
...  

eLife ◽  
2015 ◽  
Vol 4 ◽  
Author(s):  
Nicolas Aznar ◽  
Krishna K Midde ◽  
Ying Dunkel ◽  
Inmaculada Lopez-Sanchez ◽  
Yelena Pavlova ◽  
...  

Wnt signaling is essential for tissue homeostasis and its dysregulation causes cancer. Wnt ligands trigger signaling by activating Frizzled receptors (FZDRs), which belong to the G-protein coupled receptor superfamily. However, the mechanisms of G protein activation in Wnt signaling remain controversial. In this study, we demonstrate that FZDRs activate G proteins and trigger non-canonical Wnt signaling via the Dishevelled-binding protein, Daple. Daple contains a Gα-binding and activating (GBA) motif, which activates Gαi proteins and an adjacent domain that directly binds FZDRs, thereby linking Wnt stimulation to G protein activation. This triggers non-canonical Wnt responses, that is, suppresses the β-catenin/TCF/LEF pathway and tumorigenesis, but enhances PI3K-Akt and Rac1 signals and tumor cell invasiveness. In colorectal cancers, Daple is suppressed during adenoma-to-carcinoma transformation and expressed later in metastasized tumor cells. Thus, Daple activates Gαi and enhances non-canonical Wnt signaling by FZDRs, and its dysregulation can impact both tumor initiation and progression to metastasis.


2020 ◽  
Vol 11 ◽  
pp. 204062232090199 ◽  
Author(s):  
Anqing Huang ◽  
Yuli Huang

Secreted frizzled-related proteins (Sfrps) are a family of secreted proteins that bind extracellularly to Wnt ligands and frizzled receptors. This binding modulates the Wnt signaling cascade, and Sfrps interact with their corresponding receptors. Sfrps are thought to play an important role in the pathological mechanism of cardiac disease such as myocardial infarction, cardiac remodeling, and heart failure. However, the overall role of Sfrps in cardiac disease is unknown. Some members of the Sfrps family modulate cellular apoptosis, angiogenesis, differentiation, the inflammatory process, and cardiac remodeling. In this review, we summarize the evidence of Sfrps association with cardiac disease. We also discuss how multiple mechanisms may underlie Sfrps being involved in such diverse pathologies.


2020 ◽  
Author(s):  
Shahan Mamoor

The Wnt pathway transduces signals through a series of intracellular mediators including Axin, dishevelled proteins, and through regulation of an Axin destruction complex by casein kinases to effect nuclear translocation of β-catenin and β-catenin cooperation with TCF/LEF proteins at nuclear transactivation targets following binding of Wnt ligands to Frizzled receptors which in concert with LRP co-receptors at the plasma membrane (1-3). Trastuzumab, a monoclonal antibody targeted against the human epidermal growth factor receptor 2 (HER2) is utilized for the treatment of human breast cancer (4), but a complete understanding of how tumor signal transduction is modulated by trastuzumab treatment is lacking. By mining published and public microarray and gene expression data (5-7) from the primary tumors of patients treated with trastuzumab, we found that the Wnt ligands Wnt2 and Wnt10b, molecules with the capacity to support proliferation of ventral midbrain progenitors (8) and to induce transformation of the mammary gland (9), were among the genes most differentially expressed in the primary tumors of patients treated with trastuzumab. Increased expression of Wnt2 and Wnt10b implies that the Wnt pathway may be activated in primary tumors of patients treated with trastuzumab.


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